Personal Information
Entreprise/Lieu de travail
Düsseldorf, DE Germany
Profession
Researcher
Secteur d’activité
Medical / Health Care / Pharmaceuticals
À propos
Biologist by training, I have worked at the interface of clinical research, data management and IT development
Mots-clés
clinical trials
clinical research
data sharing
clinical data management
data management
infrastructure
privacy
research
validation
computer
regulations
data
software development
learning health system
good clinical practice
legal requirements
personalized medicine
gcp
compliance
standards
cdisc
knowledge
requirements specification
ecrin
business model
evaluation
software tools
services
patient reported outcome
patients
knowledge management
implementation
computer system validation
ethical principles
analysis
data ownership
data mining
open data
patient empowerment
decision support
guidelines
service provision
integration
system
electronic data capture
legal
linked data
software
database
information objects
study protocol
biomedical research
cdash
information model
bridg
share
development
obi
pico
ocre
data integration
information
terminologies
ontologies
dataverse
figshare
dryad
zenodo
b2safe
b2share
recommendations
data privacy
data protection
data reuse
data repository
user interface
graphical interface
temporal intervals
time-stamp database
time anchor
time points
eligibility criteria
clinical sites
hospital
feasibility
patient recruitment
patient identification
query generator
query
temporal relations
usage scenarios
business interactions
domain scenario
use cases
scenario
functionality
design modification
quality
elicitation
change management
software requirement specification
consistency
stakeholder needs
requirement engineering
requirements
validation master plan
cohort study
gord
patient care
randomisation
diabetes
observational studies
safety
ehr
esource
reciprocal exchange
dna sequencing
research services
genome
interventions
quality standard
network
usability
data management system
interoperability
ercin
electronic health record
enabler
information sharing
information technology
patient-centric trials
recruitment
networks
diagnosis
genotype
epidemiology
sustainability
models
comparison
us perspective
europe
european perspective
learning
lhs
risk
gamp
edc
consent
risk management
justice
beneficence
informed choices
legal assessment tool
medical data
ethical requirements
data repositories
medical
tool integration
identifiable data
patient
regulatory
ethics
data access
21crfpart11
validation life cycle
quality management
validation policy
master plan
sop
csv
trust
service exchange
exchange
customer relationship management
service
strategy
assessment
tools
open access
biosamples
search
Tout plus
Présentations
(14)J’aime
(3)Visual Data Representation Techniques Combining Art and Design
Logo Design Guru
•
il y a 8 ans
Ways of Seeing Data: Towards a Critical Literacy for Data Visualisations as Research Objects and Devices
Jonathan Gray
•
il y a 8 ans
DAMA Webinar - Big and Little Data Quality
DATAVERSITY
•
il y a 8 ans
Personal Information
Entreprise/Lieu de travail
Düsseldorf, DE Germany
Profession
Researcher
Secteur d’activité
Medical / Health Care / Pharmaceuticals
À propos
Biologist by training, I have worked at the interface of clinical research, data management and IT development
Mots-clés
clinical trials
clinical research
data sharing
clinical data management
data management
infrastructure
privacy
research
validation
computer
regulations
data
software development
learning health system
good clinical practice
legal requirements
personalized medicine
gcp
compliance
standards
cdisc
knowledge
requirements specification
ecrin
business model
evaluation
software tools
services
patient reported outcome
patients
knowledge management
implementation
computer system validation
ethical principles
analysis
data ownership
data mining
open data
patient empowerment
decision support
guidelines
service provision
integration
system
electronic data capture
legal
linked data
software
database
information objects
study protocol
biomedical research
cdash
information model
bridg
share
development
obi
pico
ocre
data integration
information
terminologies
ontologies
dataverse
figshare
dryad
zenodo
b2safe
b2share
recommendations
data privacy
data protection
data reuse
data repository
user interface
graphical interface
temporal intervals
time-stamp database
time anchor
time points
eligibility criteria
clinical sites
hospital
feasibility
patient recruitment
patient identification
query generator
query
temporal relations
usage scenarios
business interactions
domain scenario
use cases
scenario
functionality
design modification
quality
elicitation
change management
software requirement specification
consistency
stakeholder needs
requirement engineering
requirements
validation master plan
cohort study
gord
patient care
randomisation
diabetes
observational studies
safety
ehr
esource
reciprocal exchange
dna sequencing
research services
genome
interventions
quality standard
network
usability
data management system
interoperability
ercin
electronic health record
enabler
information sharing
information technology
patient-centric trials
recruitment
networks
diagnosis
genotype
epidemiology
sustainability
models
comparison
us perspective
europe
european perspective
learning
lhs
risk
gamp
edc
consent
risk management
justice
beneficence
informed choices
legal assessment tool
medical data
ethical requirements
data repositories
medical
tool integration
identifiable data
patient
regulatory
ethics
data access
21crfpart11
validation life cycle
quality management
validation policy
master plan
sop
csv
trust
service exchange
exchange
customer relationship management
service
strategy
assessment
tools
open access
biosamples
search
Tout plus